Ragge, N.
57  results:
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1

371 A Single-Centre Impact Assessment of Delayed Imaging in..:

Beder, D ; Hassan, M ; Khan, T...
British Journal of Surgery.  110 (2023)  Supplement_7 - p. , 2023
 
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CONGENITAL MUSCULAR DYSTROPHIES:

Munot, P. ; McCrea, N. ; Torelli, S....
Neuromuscular Disorders.  30 (2020)  - p. S105 , 2020
 
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4

Genetics in microphthalmia:

Calvas, P. ; Davis, E. ; Ragge, N....
Acta Ophthalmologica.  94 (2016)  S256 - p. , 2016
 
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5

Specific gene in microphthalmia:

Rozet, J.M. ; Fares‐Taïe, L. ; Chassaing, N....
Acta Ophthalmologica.  94 (2016)  S256 - p. , 2016
 
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7

Chronic Dermal Sinuses As A Manifestation Of Histiocytosis :

Sacks, S. H. ; Hall, I. ; Ragge, N..
British Medical Journal (Clinical Research Edition).  292 (1986)  6528 - p. 1097-1098 , 1986
 
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11

Clinical and genetic patterns of neurofibromatosis 1 and 2:

Ragge, N K
British Journal of Ophthalmology.  77 (1993)  10 - p. 662-672 , 1993
 
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12

TRAPPC11-related muscular dystrophy with hypoglycosylation ..:

Munot, P ; McCrea, N ; Torelli, S...
https://discovery.ucl.ac.uk/id/eprint/10136721/7/Chambers_TRAPPC11-related%20muscular%20dystrophy%20with%20hypoglycosylation%20of%20alpha-dystroglycan%20in%20skeletal%20muscle%20and%20brain_VoR.pdf.  , 2022
 
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13

De novo variants in MED12 cause X-linked syndromic neurodev..:

Polla, D. L ; Bhoj, E. J ; Verheij, J. B. G. M...
Polla , D L , Bhoj , E J , Verheij , J B G M , Wassink-Ruiter , J S K , Reis , A , Deshpande , C , Gregor , A , Hill-Karfe , K , Vulto-van Silfhout , A T , Pfundt , R , Bongers , E M H F , Hakonarson , H , Berland , S , Gradek , G , Banka , S , Chandler , K , Gompertz , L , Huffels , S C , Stumpel , C T R M , Wennekes , R , Stegmann , A P A , Reardon , W , Leenders , E K S M , de Vries , B B A , Li , D , Zackai , E , Ragge , N , Lynch , S A , Cuddapah , S , van Bokhoven , H , Zweier , C & de Brouwer , A P M 2021 , ' De novo variants in MED12 cause X-linked syndromic neurodevelopmental disorders in 18 females ' , Genetics in Medicine , vol. 23 , no. 4 , pp. 645-652 . https://doi.org/10.1038/s41436-020-01040-6.  , 2021
 
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Comprehensive study of 28 individuals with SIN3A-related di..:

Balasubramanian, M ; Dingemans, AJM ; Albaba, S...
https://openaccess.sgul.ac.uk/id/eprint/113001/1/s41431-020-00769-7.pdf.  , 2021
 
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The contribution of X-linked coding variation to severe dev..:

Martin, HC ; Gardner, EJ ; Samocha, KE...
https://discovery.ucl.ac.uk/id/eprint/10121927/1/s41467-020-20852-3.pdf.  , 2021
 
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